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Symbol Name ID |
Hyls1
HYLS1, centriolar and ciliogenesis associated MGI:1924082 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Severe hydrocephalus |
Abnormal cortical gyration |
Agenesis of corpus callosum |
Absent septum pellucidum |
Anencephaly |
Arrhinencephaly |
Gray matter heterotopia |
| Disease(s) Associated with HYLS1 | ||||||||
| hydrolethalus syndrome 1 |
| Mouse Phenotypes | decreased prepulse inhibition |
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| Availability | Mouse Genotype | |
| Hyls1em1(IMPC)Tcp/Hyls1+ | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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